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. Author manuscript; available in PMC: 2010 Sep 24.
Published in final edited form as: J Phys Chem B. 2009 Sep 24;113(38):12773–12781. doi: 10.1021/jp903554n

Table 1.

Reactions and rate constants relevant to the generation and combination of dG(-H) and CH3 radicalsa

N kn (M−1 s−1)
1 S2O82- + → 2 SO4•– φ308 = 0.55 (ref. 32)
2 SO4•– + SO4•– → S2O82- (1.1±0.1)×109 (ref. 33)
3 SO4•– + dG → SO42– + dG(-H) + H+ (4.1±0.3)×109b
4 SO4•– + DMSO ⇆ [SO4•–... DMSO] 1×1010b,c
(2.1±0.2)×107b,d
5 [SO4•–... DMSO] + H2O → SO42– + CH3 + H3CSO2H + H+ (4.2±0.4)×106b,e
6 dG + [SO4•–... DMSO] → dG(-H) + SO42– + DMSO (3.8±0.4)×109b
7 dG(-H) + CH3 → Me-dG (4.7±0.8)×108b
8 CH3 + CH3 → C2H6 (1.6±0.2)×109 (ref. 34)
9 dG(-H) + dG(-H) → products (1.0±0.1)×108b
a

25 mM deoxygenated phosphate buffer solution, pH 7.4.

b

obtained in this work.

c

the rate constant for complex formation, k4.

d

The rate constant for complex dissociation, k−4 is in units of s−1.

e

rate constant for CH3 radical formation, k5 (in units of s−1).